Raven P W, McAuley M E, Vinson G P
J Endocrinol. 1983 Oct;99(1):13-22. doi: 10.1677/joe.0.0990013.
The finding that incubation of rat adrenal capsules (largely zona glomerulosa) with trypsin reproducibly releases aldosterone and 18-hydroxycorticosterone (18-OH-B) from tightly protein-bound tissue stores leads to the hypothesis that the secretion of these steroids may be under the control of endogenous proteases. Rat adrenal capsule whole tissue and collagenase-dispersed cells were incubated under conditions of stimulation by (1-24)ACTH (10(-7) mol/l), potassium (8.4 X 10(-3) mol/l) or dibutyryl cyclic AMP (dbcAMP) (10(-4) mol/l) with the addition in some flasks of one of the following protease inhibitors at the appropriate concentration for their known actions: N alpha-p-tosyl-L-arginine methyl ester (TAME; 10(-2) mol/l), 2-nitro-4-carboxyphenyl-N,N'-diphenylcarbamate (NCDC; 2 X 10(-6) mol/l), N alpha-benzoyl-L-arginine (BA; 10(-2) mol/l), p-nitrophenyl-N alpha-benzyloxycarbonyl-L-lysinate (CBZ-NL; 2 X 10(-6) mol/l) and soybean trypsin inhibitor (STI; 1 mg/ml). The (1-24)ACTH-stimulated steroid output in dispersed cells was not affected by NCDC, BA or CBZ-NL. However, all of the inhibitors except STI produced selective effects on aldosterone and 18-OH-B production by whole capsule tissue under certain conditions. Thus TAME and NCDC significantly inhibited the dbcAMP-stimulated production of these two steroids (aldosterone values decreased from 328 +/- 35 to 128 +/- 15 and 157 +/- 32 ng/gland pair respectively) and furthermore NCDC elicited the same effect in potassium- or ACTH-stimulated whole tissue (e.g. in K+-stimulated tissue aldosterone decreased from 79 +/- 15 to 40 +/- 7 ng/gland pair). The reverse effect was shown by BA and CBZ-NL in potassium-stimulated whole tissue, and yields of aldosterone and 18-OH-B were significantly enhanced (aldosterone increased from 79 +/- 15 ng/pair to 151 +/- 14 ng in the presence of BA). The high molecular weight inhibitor STI had no effect on potassium-stimulated whole tissue, but enhanced the yield of extractable aldosterone from 9.7 +/- 1.7 to 16.9 +/- 2.3 ng/pair when added to incubations of a cytosol preparation. The results suggest that endogenous proteases in rat adrenal whole capsule tissue play specific roles in the control of aldosterone and 18-OH-B secretion. Some (type 1) whose action is mimicked by trypsin, are inhibited by TAME and NCDC and appear to be involved in the release of these two steroids from their tight (apparently covalent) binding to protein.(ABSTRACT TRUNCATED AT 400 WORDS)
将大鼠肾上腺被膜(主要是球状带)与胰蛋白酶一起孵育,可重复性地从紧密结合蛋白的组织储存中释放醛固酮和18 - 羟皮质酮(18 - OH - B),这一发现引发了如下假说:这些类固醇的分泌可能受内源性蛋白酶的控制。将大鼠肾上腺被膜全组织和经胶原酶分散的细胞在(1 - 24)促肾上腺皮质激素(ACTH)(10⁻⁷mol/L)、钾(8.4×10⁻³mol/L)或二丁酰环磷腺苷(dbcAMP)(10⁻⁴mol/L)刺激的条件下孵育,在一些培养瓶中加入以下蛋白酶抑制剂之一,其浓度适合已知作用:Nα - 对甲苯磺酰 - L - 精氨酸甲酯(TAME;10⁻²mol/L)、2 - 硝基 - 4 - 羧基苯基 - N,N' - 二苯基氨基甲酸盐(NCDC;2×10⁻⁶mol/L)、Nα - 苯甲酰 - L - 精氨酸(BA;10⁻²mol/L)、对硝基苯基 - Nα - 苄氧羰基 - L - 赖氨酸盐(CBZ - NL;2×10⁻⁶mol/L)和大豆胰蛋白酶抑制剂(STI;1mg/ml)。分散细胞中(1 - 24)ACTH刺激的类固醇分泌不受NCDC、BA或CBZ - NL的影响。然而,除STI外,所有抑制剂在某些条件下对肾上腺被膜全组织中醛固酮和18 - OH - B的产生均产生选择性作用。因此,TAME和NCDC显著抑制dbcAMP刺激的这两种类固醇的产生(醛固酮值分别从328±35降至128±15和157±32ng/腺体对),此外,NCDC在钾或ACTH刺激的全组织中也产生相同作用(例如在钾刺激的组织中,醛固酮从79±15降至40±7ng/腺体对)。BA和CBZ - NL在钾刺激的全组织中表现出相反的作用,醛固酮和18 - OH - B的产量显著增加(在BA存在下,醛固酮从79±15ng/对增加到151±14ng)。高分子量抑制剂STI对钾刺激的全组织无作用,但当添加到胞质溶胶制剂的孵育物中时,可将可提取醛固酮的产量从9.7±1.7提高到16.9±2.3ng/对。结果表明,大鼠肾上腺全被膜组织中的内源性蛋白酶在醛固酮和18 - OH - B分泌的控制中起特定作用。一些(1型)其作用被胰蛋白酶模拟,被TAME和NCDC抑制,似乎参与了这两种类固醇从与蛋白质紧密(显然是共价)结合中的释放。(摘要截短至400字)